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CS-W001157 4
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8-Bromo-4-chloro-6-methylquinoline

  • CAS No. 1156602-22-0

  • Cat. No. CS-0200434
  • Purity≥98%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

8-Bromo-4-chloro-6-methylquinoline|CS-0200434

Structure of 1156602-22-0

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General Information

  • CAS No. 1156602-22-0
  • Cat. No. CS-0200434
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₇BrClN
  • Molecular Weight 256.53
  • Synonym(s) None
  • SMILES CC1=CC(Br)=C2N=CC=C(Cl)C2=C1

Description

8-Bromo-4-chloro-6-methylquinoline is a halogenated quinoline derivative featuring strategic substitution at the 8, 4, and 6 positions. This electron-deficient scaffold integrates bromine and chlorine moieties for downstream cross-coupling, while the methyl group enhances solubility and steric profile. The compound serves as a key building block in medicinal chemistry and materials science.

Application

8-Bromo-4-chloro-6-methylquinoline serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted quinoline scaffolds via Pd-catalyzed cross-coupling reactions. The strategically positioned bromo and chloro groups exhibit complementary reactivity, facilitating sequential functionalization while maintaining stability under standard reaction conditions. Its methyl group enhances lipophilicity and provides a handle for further derivatization, making it well-suited for the synthesis of bioactive heterocycles and API intermediates.

Safety Information

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GHS Pictogram :
GHS No : GHS05,GHS06
Signal Word : Danger
UN#: 2811
Class : 6.1
Packing Group : Ⅲ
Hazard Statements : H301-H318
Precautionary Statements : P264-P270-P330-P405-P501

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Computational Chemistry Data

  • TPSA   12.89
  • LogP   3.95912
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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